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Completed Not applicable Interventional Results available

Fluid Management of Acute Decompensated Heart Failure Subjects Treated With Reprieve Decongestion Management System (DMS)

ClinicalTrials.gov ID: NCT05174312

Public ClinicalTrials.gov record NCT05174312. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 3:47 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Fluid Management of Acute Decompensated Heart Failure Subjects Treated With Reprieve Decongestion Management System (DMS) - FASTR Trial

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this study is to prospectively compare decongestive therapy administered by the Reprieve DMS system to Optimal Diuretic Therapy (ODT) in the treatment of patients diagnosed with acute decompensated heart failure (ADHF). The main objective is to determine if the Reprieve DMS can more efficiently decongest ADHF patients in comparison to Control Therapy.

Study identification

NCT ID
NCT05174312
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Reprieve Cardiovascular, Inc
Industry
Enrollment
100 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 11, 2022 (Actual)
Primary completion
Jan 10, 2025 (Actual)
Completion
Jan 10, 2025 (Actual)
Last update posted
Jun 23, 2026

2022 – 2025

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
15
Facility City State ZIP Site status
Eastern Shore Research Institute Fairhope Alabama 36532 —
University of California Irvine Irvine California 92697 —
MedStar Washington Hospital Center Washington D.C. District of Columbia 20010 —
Trinity Health Ann Arbor Hospital Ypsilanti Michigan 48197 —
St. Louis VA St Louis Missouri 63130 —
Washington University St Louis Missouri 63130 —
Duke University Hospital Durham North Carolina 27710 —
Cone Health Greensboro North Carolina 27401 —
Atrium Health Wake Forest Baptist Medical Center Winston-Salem North Carolina 27157 —
The Lindner Research Center at Christ Hospital Cincinnati Ohio 45219 —
Ohio State University Hospital Columbus Ohio 43210 —
Medical University of South Carolina Charleston South Carolina 29425 —
Prisma Health Columbia South Carolina 29203 —
Ascension Texas Cardiovascular Austin Texas 78705 —
Baylor Scott & White Dallas Texas 75246 —
University of Vermont Medical Center Burlington Vermont 05401 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05174312, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 23, 2026 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05174312 live on ClinicalTrials.gov.

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